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临床试验/NCT07657338
NCT07657338尚未招募不适用

Effects of Chinese Herbal Medicine as an Adjunctive Therapy on Renal Function in Patients With Non-Diabetic Chronic Kidney Disease: A Pilot Randomized Controlled Trial

China Medical University Hospital1 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2026年6月11日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
66
试验地点
1

研究概览

简要总结

This study is a randomized controlled pilot trial designed to evaluate the effects and safety of a traditional Chinese medicine formula (CKD-1) as an add-on therapy to standard treatment in patients with stage 3-4 non-diabetic chronic kidney disease. Eligible participants will be randomly assigned to receive either standard care alone or standard care combined with CKD-1 for 12 weeks. Kidney function, urine protein levels, and quality of life will be assessed before and after the intervention. The study aims to provide preliminary evidence on whether CKD-1 can improve renal function and quality of life in this patient population.

详细描述

This study is a prospective, single-blind (data analyst-blinded), randomized controlled pilot trial evaluating a traditional Chinese medicine formula (CKD-1) as adjunctive therapy in patients with stage 3-4 non-diabetic chronic kidney disease. Chronic kidney disease is a progressive condition with limited treatment options to slow renal deterioration. Traditional Chinese medicine is widely used as a complementary approach, but clinical evidence remains limited. This trial is designed to provide preliminary clinical evidence on the potential role of CKD-1 in improving renal outcomes and supporting future large-scale randomized controlled trials.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

盲法说明

Although this study is open-label, the data analysts performing statistical analyses and interpreting the results will remain blinded to group allocation throughout the study to minimize analysis and interpretation bias.

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adults aged ≥18 years.
  • Patients diagnosed with stage 3-4 chronic kidney disease (CKD), confirmed by a nephrologist and classified as ICD-10-CM codes N18.3-N18.
  • Ability to understand the study procedures and provide written informed consent.
  • Willingness to comply with study procedures and follow-up visits.

排除标准

  • Acute kidney injury or major kidney-related surgery within 3 months prior to enrollment.
  • Participation in another clinical trial within 3 months that may affect renal function.
  • Alanine aminotransferase (ALT) levels greater than 3 times the upper limit of normal.
  • Pregnancy or breastfeeding.
  • History of diabetes mellitus.
  • Malignancy currently receiving chemotherapy, radiotherapy, or other systemic anticancer treatment.
  • End-stage disease defined under palliative care regulations.
  • Known allergy to any components of the CKD-1 herbal formula, including Astragalus membranaceus, Salvia miltiorrhiza, Poria cocos, Moutan cortex, Scutellaria baicalensis, Lonicera japonica, or Alisma orientale.

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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